SR2S15N8 Luminous substance emitting red and light source comprising a luminous substance of said king and method for producing the luminous substance

ABSTRACT

A red-emitting luminescent material that belongs to the class of nitridosilicates and is doped with at least one activator D, in particular Eu, wherein the material is a modified D-doped alkaline earth nitridosilicate M 2 Si 5 N 8 , where M=one or more elements belonging to the group Sr, Ca, Ba, with the nitridosilicate having been stabilized by an oxidic or oxinitridic—in particular alkaline earth—phase

TECHNICAL FIELD

The invention proceeds from a red-emitting luminescent material belonging to the class of nitridosilicates according to the preamble of claim 1. The invention relates further to a light source having a luminescent material of such kind and to a method for producing the luminescent material. The light source is in particular a conversion LED. Luminescent materials of such kind are intended particularly for use in white LEDs.

PRIOR ART

WO 01/40403 shows a conversion LED that employs a red-emitting luminescent material belonging to the class of nitridosilicates. The material concerned is the luminescent material MxSiyNz:Eu, with M being represented by Ca, Sr, Ba, and/or Zn. What therein applies is that z=2/3x+4/3y. The foremost representatives are M₂Si₅N₈:Eu and MSi₇N₃:Eu.

DESCRIPTION OF THE INVENTION

The object of the present invention is to disclose a red-emitting luminescent material that is characterized by a high degree of stability so is well suited for use also in thermally stressed environments. A further object is to disclose a light source that has a luminescent material possessing those properties and a method for producing the luminescent material.

Said objects are achieved by means of the characterizing features of claim 1 or, as the case may be, 6 or, as the case may be, 14.

Particularly advantageous embodiments can be found in the claims dependent thereon.

The novel luminescent material is a modified, preferably Eu²⁺-doped, alkaline earth nitridosilicate M₂Si₅N₆, where M=one or more elements belonging to the group Sr, Ca, Ba, with the nitridosilicate having been stabilized by an oxidic—in partitular alkaline earth-phase. The luminescent material will thereby ensure the provision of an efficient, stabilized emitting red luminescent material that can be excited by blue or ultraviolet light and has a dominant wavelength in the 600-nm range.

The Eu²⁺-doped alkaline earth nitridosilicates M₂Si₅N₈, where M=one or more elements belonging to the group Sr, Ca, Ba, are a red-emitting luminescent-material system that has been known for quite a long time. However, Sr₂Si₅N₈ in particular, which is extremely interesting on account of its dominant wavelength of approximately 600 nm-610 nm, is limited in its applications owing to its chemical instability at higher temperatures (>100° C.) and when oxidized and exposed to high radiation.

While exhibiting no weaknesses in terms of emission stability, a competing system such as that of CaAlSiN₃ is precluded from many applications on account of its narrow useful range of emission wavelengths from 615 nm to 620 nm.

Thus to date no totally satisfactory solution is known for a red-emitting luminescent material system that exhibits a high degree of stability even when subjected to high temperatures.

M₃N₂, Si₃N₄, and Eu₂O₃ are needed as starting substances for preparing known M₂Si₅N₈. A novel stabilized alkaline earth nitridosilicate is obtained by extending the educt side at least to include SiO₂. The result is an initial mixture that stoichiometrically no longer yields M₂Si₅N₈ but is instead a modified Eu²⁺-doped alkaline earth nitridosilicate M₂Si₅N₈, where M=one or more elements belonging to the group Sr, Ca, Ba, with the nitridosilicate having been stabilized at least by a second oxidic phase, in particular by SiO₂. In particular the educt side has been extended to include SiO₂ and additional M₃N₂.

In a specific embodiment variant the resulting product conforms to stoichiometry (1-a)(M₂Si₅N₈:Eu)*a(SiO₂), with its preferably being the case that 0<a<0.25.

In another specific embodiment variant the resulting product conforms to stoichiometry (1-a-b)(M₂Si₅N₈:Eu)*a(SiO₂)*b(M′₃N₂), with its preferably being the case that 0<a<0.25 and 0≦b≦0.30. M′ is in particular therein different from the M used, for example M=Sr and M′=Ca. In particular, a and b are therein selected such as ultimately to yield a product in the form (M₂Si₅N₈:Eu)*(W₃Si₂O₄N₂:Eu) (M′=one or more elements belonging to the group Sr, Ca, Ba).

Generally, though, it is not simple stoichiometry that results as the product; rather it is the case that for describing the product a phase diagram has to be used that is based on the three partial components SiN_(4/3), SiO₂, and MN_(2/3).

M is preferably therein represented by Sr at over 50 mol. %

The percentage share of the entire doping means, here in particular Eu, of M ought generally to be in the 0.1-to-15-mol.-% range. Another or an additional doping agent such as, for example, Ce or Mn is not precluded. In particular, interesting systems are Eu, Mn on the one hand and Ce, Li (with or without Eu) on the other. Zi serves in the latter instance to provide charge compensation.

The luminescent material is suitable in particular for photonic excitation by a light source. Such sources are, for example, lamps such as fluorescent lamps or high-pressure discharge lamps, but in particular also conversion LEDs. The luminescent material can here be used in particular for generating white light. The RGB principle is therein usually applied. The inventive luminescent material is therein used for the red emission. Another luminescent material such as, for instance, a sion, in particular Ba sion as known per se, is used for the green emission. For the blue emission, what is best suited is the primary radiation of a blue-emitting LED; a peak wavelength of 410 to 500 nm is preferred.

A blue luminescent material such as BAM can additionally be used in the case of a peak wavelength of 410 to 430 nm. Excitation can in the case of long-wave excitation in the 470-to-500-nm range be provided by another luminescent material's secondary radiation.

The relative percentage shares of the phase triangle SiN_(4/3), SiO₂, MN_(2/3) are preferably in a range having the following key points, with the sum in each case adding to 100 mol. %:

SiO₂:SiN_(4/3):MN_(2/3)=7.5%:97.5%:25%  (1)

SiO₂:SiN_(4/3):MN_(2/3)17.5%:57.5%:25%  (2)

SiO₂:SiN_(4/5):MN_(2/3)=7.5%:47.5%:45%  (3)

SiO₂:SiN_(4/3):MN_(2/3)17.5%:37.5%:45%.  (4)

What applies particularly preferably is:

SiO₂:SiN_(4/3):MN_(2/3)10%:65%:25%  (1)

SiO₂:SiN_(4/3):MN_(2/3)15%:60%:25%  (2)

SiO₂:SiN_(4/5):MN_(2/3)10%:45%:45%  (3)

SiO₂:SiN_(4/3):MN_(2/3)15%:40%:45%.  (4)

SHORT DESCRIPTION OF THE DRAWINGS

The invention is described in more detail below with the aid of several exemplary embodiments:

FIG. 1 is a phase diagram that localizes known and novel stabilized nitridosilicates;

FIG. 2 is a powder diffractogram of a known nitridosilicate Sr₂Si₅N₈:Eu;

FIG. 3 is a powder diffractogram of a stabilized nitridosilicate Sr₂Si₅N₈:Eu*nSiO₂;

FIG. 4 shows the relative loss of quantum efficiency after an oxidation test for the two luminescent materials shown in FIGS. 2 and 3;

FIG. 5 shows the result of a stress test using a high irradiation strength for the two luminescent materials shown in FIGS. 2 and 3;

FIG. 6 shows the measurement of the quenching characteristics for the two luminescent materials shown in FIGS. 2 and 3 as a function of temperature;

FIG. 7 shows the excitability of various luminescent materials as a function of wavelength;

FIG. 8 shows the loss of efficiency of a conversion LED as a function of time;

FIG. 9 is a schematic of a conversion LED;

FIG. 10 shows the converter loss in percentage terms for a stabilized nitride;

FIG. 11 shows the converter loss in percentage terms for a non-stabilized nitride;

FIG. 12 shows the spectrum for an LED having a stabilized nitride;

FIG. 13 shows the spectrum for an LED having a non-stabilized nitride.

PREFERRED EMBODIMENT VARIANT OF THE INVENTION

Exemplary embodiments of the novel red-emitting luminescent material are as follows. The resulting dominant emission wave-length is therein in the 595-to-6.0-nm range.

a) Initial mixture 1, normal nitridosilicate

8.7 g Sr₃N₂, 10.9 g Si₃N₄, and 0.3 g Eu₂O₃ are weighed-in in a protective-gas atmosphere and homogenized. The educt mixture is then roasted in the tube or chamber furnace for several hours in a reducing atmosphere at temperatures of between 1,200° C. and 1,800° C. That can be followed by a second roasting, likewise in a reducing atmosphere, at between 1,200° C. and 1,800° C.

b) Initial mixture 2, stabilized nitridosilicate

10.9 g Sr₃N₂, 1.7 g SiO₂, 6.8 g Si₃N₄, and 0.4 g Eu₂O₃ are weighed-in in a protective-gas atmosphere and homogenized. The educt mixture is then roasted in the tube or chamber furnace for several hours in a reducing atmosphere at temperatures of between 1,200° C. and 1,800° C. That can be followed by a second roasting, likewise in a reducing atmosphere, at between 1,200° C. and 1,800*C.

c) Initial mixture 3, stabilized nitridosilicate

11.5 g Sr₃N₂, 0.9 g SiO₂, 7.2 g Si₃N₄, and 0.4 g Eu₂O₃ are weighed-in in a protective-gas atmosphere and homogenized. The educt mixture is then roasted in the tube or chamber furnace for several hours in a reducing atmosphere at temperatures of between 1,200° C. and 1,800° C. That can be followed by a second roasting, likewise in a reducing atmosphere, at between 1,200° C. and 1,800° C.

d) Initial mixture 4, stabilized nitridosilicate

10.7 g Sr₃N₂, 2.2 g SiO₂, 6.7 g Si₃N₄, and 0.4 g Eu₂O₃ are weighed-in in a protective-gas atmosphere and homogenized. The educt mixture is then roasted in the tube or chamber furnace for several hours in a reducing atmosphere at temperatures of between 1,200° C. and 1,800° C. That can be followed by a second roasting, likewise in a reducing atmosphere, at between 1,200° C. and 1,800° C.

e) Initial mixture 5, stabilized nitridosilicate

8.8 g Sr₃N₂, 1.2 g Ca₃N₂, 2.7 g SiO₂, 6.9 g Si₃N₄, and 0.4 g Eu₂O₃ are weighed-in in a protective-gas atmosphere and homogenized. The educt mixture is then roasted in the tube or chamber furnace for several hours in a reducing atmosphere at temperatures of between 1,200° C. and 1,800° C. That can be followed by a second roasting, likewise in a reducing atmosphere, at between 1,200° C. and 1,800° C.

TABLE 1 Color point, quantum efficiency, brightness Eu Rel. Rel. (mol. λ_(dom) Λ_(eff) Q.E. brightness Sample Initial %) x y (nm) (nm) (%) (%) BP 001/07 1 2 0.627 0.371 600.3 635.2 100 100 BP 047/07 2 2 0.627 0.372 600.1 631.2 101 105 KO BP 075/07 3 2 0.626 0.373 599.9 631.2 95 101 BP 084/07 4 2 0.626 0.372 600.1 631.6 101 105 BP 059/08 5 2 0.638 0.361 602.6 644.1 103 112

Proceeding generally from the M₂Si₅N₈ point toward the dashed line, we find the quantum efficiency will first drop dramatically before climbing again at the marked region's boundary. That is illustrated by way of example with M=Sr. M is here preferably predominantly more than 50 mol. %, particularly preferably M=Sr. The percentage share of Eu in M is preferably 0.1 to 15 mol. %. The exemplary region having the key points—which region is identified in the phase triangle by the dashed line—is therefore preferably (the associated stoichiometry is indicated in parentheses):

-   (1) SiO₂:SiN_(4/3):SrN_(2/3)=7.5%:67.5%:25%     (Sr_(2.5)Si_(7.5)O_(1.5)N_(10.67)) -   (2) SiO₂:SiN_(4/3):SrN_(2/3)=17.5%:57.5%:25%     (Sr_(2.5)Si_(7.5)O_(3.5)N_(9.33)) -   (3) SiO₂:SiN_(4/3):SrN_(2/3)=7.5%:47.5%:45%     (Sr_(4.5)Si_(5.5)O_(1.5)N_(9.33)) -   (4) SiO₂:SiN_(4/3):SrN_(2/3)=17.5%:37.5%:45%     (Sr_(4.5)Si_(5.5)O_(3.5)N₈),     which is characterized by a relative loss of <40% in terms of the     quantum efficiency of the best stabilized Sr₂Si₅N₈ sample.

Having quantum efficiencies of more than 70%, the region identified by the unbroken line is to be given particular preference. The rectangle is here described by the following key points:

(A) SiO₂:SiN_(4/3):SrN_(2/3)=10%:65%:25% (Sr_(2.5)Si_(7.5)O₂N_(10.33)) (B) SiO₂:SiN_(4/3):SrN_(2/3)=15%:60%:25% (Sr_(2.5)Si_(7.5)O₂N₉) (C) SiO₂:SiN_(4/3):SrN_(2/3)=10%:45%:45% (Sr_(4.5)Si_(5.5)O₂N₉) (D) SiO₂:SiN_(4/3):SrN_(2/3)=15%:40%:45% (Sr_(4.5)Si_(5.5)O₃N_(8.33))

TABLE 2 Positions of the most important reflexes of the novel phase 2theta/TOF No. (+/−0.2) I_(obs) 1 22.7 Weak 2 24.8 Weak 3 29.6 Weak 4 32.4 Strong 5 39.9 Medium 6 46.5 Medium 7 52.2 Weak 8 57.7 Medium

Adding SiO₂ to the initial mixture results in a second phase that significantly improves the luminescent material M₂Si₅N_(8:)D—with D being represented preferably by Eu—in terms of all its limiting characteristics while not weakening it in any of its characteristics. The resulting ancillary phase is a hitherto unknown, probably oxinitridic phase, which according to current knowledge crystallizes in the structure of Ba₃Al₂O₆ (space group Pa 3 (No. 205) and lattice parameter a 15.650(1)A).

FIG. 7 shows differences in the normal and stabilized nitridosilicate's excitability. While the excitability of stabilized Eu-doped Sr₂Si₅N₈ breaks down at an excitation wavelength of 360 nm more intensely than that of normal Sr₂Si₅N₈, the former has significantly better excitability between 410 and 500 nm, which is advantageous specifically in the case of excitation by a blue LED chip.

Sr₂Si₅N₈, which is unstable in all respects and whose dominant emission wavelength of approximately 600-610 nm is favorable for numerous applications, can be stabilized in all the above aspects (temperature quenching, laser stability, oxidation stability) without detriment to its optical properties.

FIG. 2 is the powder diffractogram of Sr nitridosilicate Sr₂Si₅N₈:Eu as known per se. By contrast, the powder diffractogram of modified SiO₂-stabilized Sr₂Si₅N₈:Eu shown in FIG. 3 exhibits totally different peaks.

FIG. 4 shows the relative loss of quantum efficiency for normal and modified Sr nitridosilicate as shown in FIGS. 2 and 3.

FIG. 5 shows the stability for normal and modified Sr nitridosilicate as shown in FIGS. 2 and 3 when exposed to a high level of laser radiation. The exposure length is therein indicated as an abscise. The ordinate shows the relative intensity of the radiation.

FIG. 6 shows temperature quenching for normal and modified Sr nitridosilicate as shown in FIGS. 2 and 3. The abscise is therein the temperature in degrees Celsius and the ordinate is the brightness compared with the brightness at 25° C., meaning not under temperature stress.

FIG. 7 shows the excitability of various luminescent materials as a function of excitation wavelength.

FIG. 8 shows the loss of conversion efficiency of stabilized and normal Sr₂Si₅N₈:Eu as a function of time (in hours). The length of radiation exposure is therein plotted as the abscise. The ordinate is the percentage loss.

According to FIG. 9, a conversion LED 1 has a chip 2 that emits the primary radiation. The primary radiation is most generally blue with a peak wavelength in the 420-to-480-nm, preferably 450-to-470-nm, range. It can, though, also be a UV LED, with the primary radiation most generally being in the 360-to-420-nm range.

The chip is connected to electric terminals 3 and a bond wire 14. It is surrounded by a housing 8 acting as a reflector 17. Mounted on the chip is a potting 5 containing a luminescent-material mixture 6 in dispersion form. The luminescent materials are a red-emitting luminescent material of the modified nitridosilicate type and a yellow-green luminescent material such as, for instance, YAG:Ce or a sion such as BaSi₂O₂N₂:Eu.

FIG. 10 shows as an alternative an exemplary embodiment in which a plurality of LEDs 16 are accommodated together with an electronic control 17 in a module 15 having a baseplate 18 and walls 19. The luminescent material is here applied to the inside of the walls or only on cover plate 20.

FIG. 11 shows the converter loss as a function of time for a stabilized nitride in which a=b. M=Sr and M′=Sr, Ca therein. Stabilizing is much better than in the case of a non-stabilized customary nitride whose converter loss (as a percentage) is shown in FIG. 12.

FIG. 13 shows the spectrum of an LED having a stabilized nitride at the beginning and after ageing. The stability is much greater than in the case of the spectrum shown in the comparison (see FIG. 14) of an LED having a non-stabilized nitride.

TABLE 3 Color point, quantum efficiency, brightness Rel. Rel. Eu λ_(dom) Λ_(wk) Q.E. brightness Sample Type (mol. %) x y (nm) (nm) (%) (%) BP 001/07 Sr₂Si₅N₈ 2 0.627 0.371 600.3 635.2 100 100 BP 047/07 Stab. 2 0.627 0.372 600.1 631.2 101 105 KO Sr₂Si₅N₈ BP 048/07 Stab. 10 0.656 0.343 607.3 656.4 90 107 KO Sr₂Si₅N₈ BP 084/07 Stab. 2 0.626 0.372 600.1 631.6 101 105 Sr₂Si₅N₈ BP 084a/07 Stab. 2 0.626 0.372 600.1 632.6 98 107 Sr₂Si₅N₈ BP 059/08 Stab. 2 0.638 0.361 602.6 644.1 103 112 (Sr_(0.8)Ca_(0.2))₂ Si₅N₈

TABLE 4 Changes after oxidation test (68 h at 150° C. in air atmosphere) BP 001/07 BP 047/07 KO Sr₂Si₅N₈ Stab. Sr₂Si₅N₈ Before After Before After ox. test ox. test ox. test ox. test Rel. quantum 100 79.8 100 94.7 efficiency (%) Color point x/y 0.627/ 0.626/ 0.627/ 0.626/ 0.371 0.372 0.372 0.372 Dominant 600.3 600.1 600.1 600.1 wavelength (nm) Effective wavelength 635.2 634.5 631.2 631.2 (nm) Brightness rel. to 100 76.0 100 89.5 standard (%) 

1. A red-emitting luminescent material that belongs to the class of nitridosilicates and is doped with at least one activator D, wherein the material is a modified D-doped alkaline earth nitridosilicate M₂Si₅N₈, where M=one or more elements belonging to the group Sr, Ca, Ba, with the nitridosilicate having been stabilized by an oxidic or oxinitridic phase.
 2. The luminescent material as claimed in claim 1, wherein M is represented by Sr at over 50 mol. %.
 3. The luminescent material as claimed in claim 1, wherein the relative percentage shares of the phase triangle SiN_(4/3), SiO₂, MN_(2/3) are in a range having the following key points: (1) SiO₂:SiN_(4/3):MN_(2/3)=7.5%:67.5%:25% (2) SiO₂:SiN_(4/3):MN_(2/3)=17.5%:57.5%:25% (3) SiO₂:SiN_(4/3):MN_(2/3)=7.5%:47.5%:45% (4) SiO₂:SiN_(4/3):MN_(2/3)=17.5%:37.5%:45%.
 4. The luminescent material as claimed in claim 1, wherein the relative percentage shares of the phase triangle SiN_(4/3), SiO₂, MN_(2/3) are in a range having the following key points: (1) SiO₂:SiN_(4/3):MN_(2/3)=10%:65%:25% (2) SiO₂:SiN_(4/3):MN_(2/3)=15%:60%:25% (3) SiO₂:SiN_(4/3):MN_(2/3)=10%:45%:45% (4) SiO₂:SiN_(4/3):MN_(2/3)=15%:40%:45%.
 5. The luminescent material as claimed in claim 1, wherein the percentage share of the activator D of M is in the 0.1-to-15-mol.-% range.
 6. The luminescent material as claimed in claim 1, wherein the stabilized luminescent material exhibits stoichiometry (1-ab)(M₂Si₅N₈:D)*a(SiO₂)*b(M′₃N₂).
 7. A conversion LED, having a luminescent material as claimed in claim
 1. 8. The conversion LED as claimed in claim 7, wherein the conversion LED emits white light.
 9. The conversion LED as claimed in claim 7, wherein the luminescent material is energized by means of radiation whose peak is in the 410-to-500-nm range.
 10. The conversion LED as claimed in claim 7, wherein the luminescent material's dominant emission wavelength is in the 595-to-610-nm range.
 11. The conversion LED as claimed in claim 7, wherein a second luminescent material that emits yellow-green light is used for a whiteemitting LED.
 12. The conversion LED as claimed in claim 7, wherein the luminescent material is integrated in the LED.
 13. The conversion LED as claimed in claim 7, wherein the luminescent material has been separately applied to a carrier.
 14. The conversion LED as claimed in claim 7, wherein the chip emits primary radiation in the UV-to-blue range, with at least one further luminescent material possibly also being used.
 15. A method for producing a red-emitting luminescent material that belongs to the class of nitridosilicates and is doped with an activator D and which is a modified doped alkaline earth nitridosilicate M₂Si₅N₅, where M=one or more elements belonging to the group Sr, Ca, Ba and where M′=one or more elements belonging to the group Sr, Ca, Ba, with the nitridosilicate having been stabilized by an oxidic or oxinitridic—phase, wherein the educts M₃N₂, Si₃N₄, SiO₂, and possibly M′₃N₂ as well as a precursor of activator D are roasted in a reducing atmosphere at temperatures of at least 1,200° C.
 16. The method of claim 15, wherein the oxidic or oxinitridic phase is an alkaline earth phase.
 17. The luminescent material of claim 1, wherein said activator D is Eu and said oxidic or oxinitridic phase is an alkaline earth phase.
 18. The conversion LED as claimed in claim 7, wherein the luminescent material is energized by means of radiation whose peak is in the 430-to-465-nm range.
 19. The conversion LED as claimed in claim 12, wherein the luminescent material is integrated in a potting compound positioned in front of a chip.
 20. The conversion LED as claimed in claim 7, wherein the chip emits primary radiation in the 360-nm-to-480-nm range, with at least one further luminescent material possibly also being used. 